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蛋白质组学能否成为未来揭示罕见神经退行性疾病发病机制的有用工具?

Could Proteomics Become a Future Useful Tool to Shed Light on the Mechanisms of Rare Neurodegenerative Disorders?

作者信息

Cagnone Maddalena, Bardoni Anna, Iadarola Paolo, Viglio Simona

机构信息

Department of Molecular Medicine, Biochemistry Unit, University of Pavia, 27100 Pavia, Italy.

Department of Biology and Biotechnologies "L. Spallanzani", Biochemistry Unit, University of Pavia, 27100 Pavia, Italy.

出版信息

High Throughput. 2018 Jan 10;7(1):2. doi: 10.3390/ht7010002.

Abstract

Very often the clinical features of rare neurodegenerative disorders overlap with those of other, more common clinical disturbances. As a consequence, not only the true incidence of these disorders is underestimated, but many patients also experience a significant delay before a definitive diagnosis. Under this scenario, it appears clear that any accurate tool producing information about the pathological mechanisms of these disorders would offer a novel context for their precise identification by strongly enhancing the interpretation of symptoms. With the advent of proteomics, detection and identification of proteins in different organs/tissues, aimed at understanding whether they represent an attractive tool for monitoring alterations in these districts, has become an area of increasing interest. The aim of this report is to provide an overview of the most recent applications of proteomics as a new strategy for identifying biomarkers with a clinical utility for the investigation of rare neurodegenerative disorders.

摘要

罕见神经退行性疾病的临床特征常常与其他更常见的临床病症重叠。因此,不仅这些疾病的真实发病率被低估,许多患者在明确诊断之前还会经历显著的延迟。在这种情况下,很明显,任何能够提供有关这些疾病病理机制信息的准确工具,都将通过有力加强症状解读,为其精确识别提供新的背景。随着蛋白质组学的出现,检测和鉴定不同器官/组织中的蛋白质,旨在了解它们是否是监测这些区域变化的有吸引力的工具,已成为一个越来越受关注的领域。本报告的目的是概述蛋白质组学作为一种新策略的最新应用,该策略用于识别具有临床效用的生物标志物,以研究罕见神经退行性疾病。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/be28/5876528/bb81507f157f/high-throughput-07-00002-g001.jpg

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